miRNAs differentially expressed in prostate cancer cell lines after soy treatment
MicroRNAs (miRNAs) are small non-coding RNAs that have aberrant expression in prostate cancer tissues. miRNAs are involved in the initiation and progression of cancer, and several miRNAs have been characterized as tumor suppressors or oncogenes. It has been shown that some miRNAs can be directly reg...
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Veröffentlicht in: | In vivo (Athens) 2011-11, Vol.25 (6), p.917-921 |
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creator | Rabiau, Nadège Trraf, Hibatullahi-Kauthar Adjakly, Mawussi Bosviel, Rémy Guy, Laurent Fontana, Luc Bignon, Yves-Jean Bernard-Gallon, Dominique J |
description | MicroRNAs (miRNAs) are small non-coding RNAs that have aberrant expression in prostate cancer tissues. miRNAs are involved in the initiation and progression of cancer, and several miRNAs have been characterized as tumor suppressors or oncogenes. It has been shown that some miRNAs can be directly regulated from their own promoters by epigenetic alterations in cancer cells. Moreover, phytoestrogens are known to have epigenetic action on gene transcription. Hence, we conducted here an examination of the miRNA expression profile in human prostate cancer cell lines after soy phytoestrogen treatment.
The comparative miRNA expression profiles of prostate cell lines (PC-3, DU145, LNCaP) after a 48-h treatment of 40 μM genistein, 110 μM daidzein, or 2 μM 5-azacytidine (5-AZA, a demethylating agent) were conducted with a Taqman low-density array.
We found that out of 377 miRNAs tested, 180, 170 and 150 miRNAs were amplified with 2% of variation in the triplicate in PC-3, DU145 and LNCap cells, respectively, and only 5 miRNAs for PC-3 and DU145 cells and 4 miRNAs for LNCap exhibited a significant change in their expression. Treatment with genistein or daidzein had similar effects on miRNA regulation to those of 5-AZA treatment.
This work demonstrated a new role of isoflavones on the regulation of miRNAs in prostate cancer. |
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The comparative miRNA expression profiles of prostate cell lines (PC-3, DU145, LNCaP) after a 48-h treatment of 40 μM genistein, 110 μM daidzein, or 2 μM 5-azacytidine (5-AZA, a demethylating agent) were conducted with a Taqman low-density array.
We found that out of 377 miRNAs tested, 180, 170 and 150 miRNAs were amplified with 2% of variation in the triplicate in PC-3, DU145 and LNCap cells, respectively, and only 5 miRNAs for PC-3 and DU145 cells and 4 miRNAs for LNCap exhibited a significant change in their expression. Treatment with genistein or daidzein had similar effects on miRNA regulation to those of 5-AZA treatment.
This work demonstrated a new role of isoflavones on the regulation of miRNAs in prostate cancer.</description><identifier>EISSN: 1791-7549</identifier><identifier>PMID: 22021684</identifier><language>eng</language><publisher>Greece</publisher><subject>Azacitidine - pharmacology ; Cell Line, Tumor ; DNA Methylation ; Genistein - pharmacology ; Humans ; Isoflavones - pharmacology ; Male ; MicroRNAs - genetics ; Prostatic Neoplasms - genetics ; Prostatic Neoplasms - pathology ; Real-Time Polymerase Chain Reaction ; Reverse Transcriptase Polymerase Chain Reaction</subject><ispartof>In vivo (Athens), 2011-11, Vol.25 (6), p.917-921</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22021684$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Rabiau, Nadège</creatorcontrib><creatorcontrib>Trraf, Hibatullahi-Kauthar</creatorcontrib><creatorcontrib>Adjakly, Mawussi</creatorcontrib><creatorcontrib>Bosviel, Rémy</creatorcontrib><creatorcontrib>Guy, Laurent</creatorcontrib><creatorcontrib>Fontana, Luc</creatorcontrib><creatorcontrib>Bignon, Yves-Jean</creatorcontrib><creatorcontrib>Bernard-Gallon, Dominique J</creatorcontrib><title>miRNAs differentially expressed in prostate cancer cell lines after soy treatment</title><title>In vivo (Athens)</title><addtitle>In Vivo</addtitle><description>MicroRNAs (miRNAs) are small non-coding RNAs that have aberrant expression in prostate cancer tissues. miRNAs are involved in the initiation and progression of cancer, and several miRNAs have been characterized as tumor suppressors or oncogenes. It has been shown that some miRNAs can be directly regulated from their own promoters by epigenetic alterations in cancer cells. Moreover, phytoestrogens are known to have epigenetic action on gene transcription. Hence, we conducted here an examination of the miRNA expression profile in human prostate cancer cell lines after soy phytoestrogen treatment.
The comparative miRNA expression profiles of prostate cell lines (PC-3, DU145, LNCaP) after a 48-h treatment of 40 μM genistein, 110 μM daidzein, or 2 μM 5-azacytidine (5-AZA, a demethylating agent) were conducted with a Taqman low-density array.
We found that out of 377 miRNAs tested, 180, 170 and 150 miRNAs were amplified with 2% of variation in the triplicate in PC-3, DU145 and LNCap cells, respectively, and only 5 miRNAs for PC-3 and DU145 cells and 4 miRNAs for LNCap exhibited a significant change in their expression. Treatment with genistein or daidzein had similar effects on miRNA regulation to those of 5-AZA treatment.
This work demonstrated a new role of isoflavones on the regulation of miRNAs in prostate cancer.</description><subject>Azacitidine - pharmacology</subject><subject>Cell Line, Tumor</subject><subject>DNA Methylation</subject><subject>Genistein - pharmacology</subject><subject>Humans</subject><subject>Isoflavones - pharmacology</subject><subject>Male</subject><subject>MicroRNAs - genetics</subject><subject>Prostatic Neoplasms - genetics</subject><subject>Prostatic Neoplasms - pathology</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><issn>1791-7549</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kE1LxDAYhIMg7rr6FyQ3T4UkTdLmuCx-waIoei5J-gYi6YdJCvbfG3E9DQzD8MycoS1tFK0awdUGXab0SYhsCGEXaMMYYVS2fIteB__2vE-4985BhDF7HcKK4XuOkBL02I94jlPKOgO2erQQsYUQcPAjJKxdLkaaVpwj6DyUgit07nRIcH3SHfq4v3s_PFbHl4enw_5YzYySXElKnCZc9bZlBZNK10JrpNMNE5YIJQQXVPaccGsIyJopUWvnqHGaWWdMvUO3f70F72uBlLvBp180PcK0pE6VubVoBS3Jm1NyMQP03Rz9oOPa_b9Q_wDK4Vhm</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Rabiau, Nadège</creator><creator>Trraf, Hibatullahi-Kauthar</creator><creator>Adjakly, Mawussi</creator><creator>Bosviel, Rémy</creator><creator>Guy, Laurent</creator><creator>Fontana, Luc</creator><creator>Bignon, Yves-Jean</creator><creator>Bernard-Gallon, Dominique J</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>20111101</creationdate><title>miRNAs differentially expressed in prostate cancer cell lines after soy treatment</title><author>Rabiau, Nadège ; Trraf, Hibatullahi-Kauthar ; Adjakly, Mawussi ; Bosviel, Rémy ; Guy, Laurent ; Fontana, Luc ; Bignon, Yves-Jean ; Bernard-Gallon, Dominique J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p210t-610fa049dc8279116f8e8b6fa725c059554516d404cb0e632953aff1bfa2cfbb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Azacitidine - pharmacology</topic><topic>Cell Line, Tumor</topic><topic>DNA Methylation</topic><topic>Genistein - pharmacology</topic><topic>Humans</topic><topic>Isoflavones - pharmacology</topic><topic>Male</topic><topic>MicroRNAs - genetics</topic><topic>Prostatic Neoplasms - genetics</topic><topic>Prostatic Neoplasms - pathology</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>Reverse Transcriptase Polymerase Chain Reaction</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rabiau, Nadège</creatorcontrib><creatorcontrib>Trraf, Hibatullahi-Kauthar</creatorcontrib><creatorcontrib>Adjakly, Mawussi</creatorcontrib><creatorcontrib>Bosviel, Rémy</creatorcontrib><creatorcontrib>Guy, Laurent</creatorcontrib><creatorcontrib>Fontana, Luc</creatorcontrib><creatorcontrib>Bignon, Yves-Jean</creatorcontrib><creatorcontrib>Bernard-Gallon, Dominique J</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>In vivo (Athens)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rabiau, Nadège</au><au>Trraf, Hibatullahi-Kauthar</au><au>Adjakly, Mawussi</au><au>Bosviel, Rémy</au><au>Guy, Laurent</au><au>Fontana, Luc</au><au>Bignon, Yves-Jean</au><au>Bernard-Gallon, Dominique J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>miRNAs differentially expressed in prostate cancer cell lines after soy treatment</atitle><jtitle>In vivo (Athens)</jtitle><addtitle>In Vivo</addtitle><date>2011-11-01</date><risdate>2011</risdate><volume>25</volume><issue>6</issue><spage>917</spage><epage>921</epage><pages>917-921</pages><eissn>1791-7549</eissn><abstract>MicroRNAs (miRNAs) are small non-coding RNAs that have aberrant expression in prostate cancer tissues. miRNAs are involved in the initiation and progression of cancer, and several miRNAs have been characterized as tumor suppressors or oncogenes. It has been shown that some miRNAs can be directly regulated from their own promoters by epigenetic alterations in cancer cells. Moreover, phytoestrogens are known to have epigenetic action on gene transcription. Hence, we conducted here an examination of the miRNA expression profile in human prostate cancer cell lines after soy phytoestrogen treatment.
The comparative miRNA expression profiles of prostate cell lines (PC-3, DU145, LNCaP) after a 48-h treatment of 40 μM genistein, 110 μM daidzein, or 2 μM 5-azacytidine (5-AZA, a demethylating agent) were conducted with a Taqman low-density array.
We found that out of 377 miRNAs tested, 180, 170 and 150 miRNAs were amplified with 2% of variation in the triplicate in PC-3, DU145 and LNCap cells, respectively, and only 5 miRNAs for PC-3 and DU145 cells and 4 miRNAs for LNCap exhibited a significant change in their expression. Treatment with genistein or daidzein had similar effects on miRNA regulation to those of 5-AZA treatment.
This work demonstrated a new role of isoflavones on the regulation of miRNAs in prostate cancer.</abstract><cop>Greece</cop><pmid>22021684</pmid><tpages>5</tpages></addata></record> |
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subjects | Azacitidine - pharmacology Cell Line, Tumor DNA Methylation Genistein - pharmacology Humans Isoflavones - pharmacology Male MicroRNAs - genetics Prostatic Neoplasms - genetics Prostatic Neoplasms - pathology Real-Time Polymerase Chain Reaction Reverse Transcriptase Polymerase Chain Reaction |
title | miRNAs differentially expressed in prostate cancer cell lines after soy treatment |
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